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病毒-细胞融合作为先天免疫的触发因素,依赖于衔接蛋白 STING。

Virus-cell fusion as a trigger of innate immunity dependent on the adaptor STING.

机构信息

Department of Biomedicine, Aarhus University, Aarhus, Denmark.

出版信息

Nat Immunol. 2012 Jun 17;13(8):737-43. doi: 10.1038/ni.2350.

Abstract

The innate immune system senses infection by detecting either evolutionarily conserved molecules essential for the survival of microbes or the abnormal location of molecules. Here we demonstrate the existence of a previously unknown innate detection mechanism induced by fusion between viral envelopes and target cells. Virus-cell fusion specifically stimulated a type I interferon response with expression of interferon-stimulated genes, in vivo recruitment of leukocytes and potentiation of signaling via Toll-like receptor 7 (TLR7) and TLR9. The fusion-dependent response was dependent on the stimulator of interferon genes STING but was independent of DNA, RNA and viral capsid. We suggest that membrane fusion is sensed as a danger signal with potential implications for defense against enveloped viruses and various conditions of giant-cell formation.

摘要

先天免疫系统通过检测微生物生存所必需的进化上保守的分子或分子的异常位置来感知感染。在这里,我们证明了一种以前未知的先天检测机制的存在,这种机制是由病毒包膜与靶细胞融合诱导的。病毒-细胞融合特异性地刺激 I 型干扰素反应,表达干扰素刺激基因,体内募集白细胞,并增强 Toll 样受体 7(TLR7)和 TLR9 的信号转导。这种融合依赖性反应依赖于干扰素基因刺激物 STING,但不依赖于 DNA、RNA 和病毒衣壳。我们认为膜融合被视为一种危险信号,可能对防御包膜病毒和各种巨细胞形成条件具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d71/3411909/ae7d6b9539b0/nihms379462f1.jpg

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